Canonical Allele Identifier: CA11102646
Gene: SH3BP4 HGNC NCBI

Linked Data

dbSNP Id: rs10174126

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.235052249T>C , CM000664.2:g.235052249T>C GRCh38
NC_000002.11:g.235960893T>C , CM000664.1:g.235960893T>C GRCh37
NC_000002.10:g.235625632T>C NCBI36
NG_033930.1:g.105266T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000392011.7:c.2479-313T>C MANE Select ENSP00000375867.2:n.2479-313T>C
ENST00000344528.8:c.2479-313T>C ENSP00000340237.4:n.2479-313T>C
ENST00000392011.6:c.2479-313T>C ENSP00000375867.2:n.2479-313T>C
ENST00000409212.5:c.2479-313T>C ENSP00000386862.1:n.2479-313T>C
NM_014521.2:c.2479-313T>C NP_055336.1:n.2479-313T>C
XM_011510891.1:c.2479-313T>C XP_011509193.1:n.2479-313T>C
XM_011510892.1:c.2479-313T>C XP_011509194.1:n.2479-313T>C
XM_011510893.1:c.2479-313T>C XP_011509195.1:n.2479-313T>C
XM_011510894.1:c.2479-313T>C XP_011509196.1:n.2479-313T>C
XM_011510891.2:c.2479-313T>C XP_011509193.1:n.2479-313T>C
XM_011510894.2:c.2479-313T>C XP_011509196.1:n.2479-313T>C
NM_014521.3:c.2479-313T>C MANE Select NP_055336.1:n.2479-313T>C
NM_001371302.1:c.2479-313T>C NP_001358231.1:n.2479-313T>C
NM_001371303.1:c.2479-313T>C NP_001358232.1:n.2479-313T>C
NM_001371304.1:c.2479-313T>C NP_001358233.1:n.2479-313T>C
NM_001371305.1:c.2479-313T>C NP_001358234.1:n.2479-313T>C
NM_001371306.1:c.2479-313T>C NP_001358235.1:n.2479-313T>C